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588 Delayed Diagnosis of Hereditary Angioedema. A Case Report
BACKGROUND: Hereditary angioedema (HAE) was first described by Quincke in 1882 and appointed by Osler in 1888, is a rare disease caused by deficiency of gene esterase inhibitor C1 (C1 INH). Prevalence varies from 1:10,000 to 1:150,000. The attacks are usually sporadic and often associated with traum...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
World Allergy Organization Journal
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3513025/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.WOX.0000411703.50677.bb |
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